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rs1878406

From SNPedia

Orientationplus
Stabilizedplus
Make rs1878406(C;C)
Make rs1878406(C;T)
Make rs1878406(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position147472512
is asnp
is mentioned by
dbSNPrs1878406
ebirs1878406
HLIrs1878406
Exacrs1878406
Varsomers1878406
Maprs1878406
PheGenIrs1878406
hapmaprs1878406
1000 genomesrs1878406
hgdprs1878406
ensemblrs1878406
gopubmedrs1878406
geneviewrs1878406
scholarrs1878406
googlers1878406
pharmgkbrs1878406
gwascentralrs1878406
openSNPrs1878406
23andMers1878406
23andMe allrs1878406
SNP Nexus

SNPshotrs1878406
SNPdbers1878406
MSV3drs1878406
GWAS Ctlgrs1878406
GMAF0.1823
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21909108OA-icon.png]
Trait
Title Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
Risk Allele T
P-val 7E-12
Odds Ratio 0.1993 [0.14-0.26] unit increase
GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele T
P-val 1E-6
Odds Ratio 1.10 [1.06-1.14]


[PMID 26520901] Impact of carotid atherosclerosis loci on cardiovascular events